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Updated: May 1, 2026

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Molecular hydrogen formation from proximal glycol pairs on TiO2(110)
Long Chen1, Zhenjun Li, R Scott Smith
1Fundamental and Computational Sciences Directorate and Institute for Integrated Catalysis, Pacific Northwest National Laboratory , P.O. Box 999, Richland, Washington 99352, United States.
Abstract:
Understanding hydrogen formation on TiO2 surfaces is of great importance, as it could provide fundamental insight into water splitting for hydrogen production using solar energy. In this work, hydrogen formation from glycols having different numbers of methyl end-groups has been studied using temperature-programmed desorption on reduced, hydroxylated, and oxidized rutile TiO2(110) surfaces. The results from OD-labeled glycols demonstrate that gas-phase molecular hydrogen originates exclusively from glycol hydroxyl groups. The yield is controlled by a combination of glycol coverage, steric hindrance, TiO2(110) order, and the amount of subsurface charge. Combined, these results show that proximal pairs of hydroxyl-aligned glycol molecules and subsurface charge are required to maximize the yield of this redox reaction. These findings highlight the importance of geometric and electronic effects in hydrogen formation from adsorbates on TiO2(110).
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